Organ sculpting by patterned extracellular matrix stiffness
- University of California-Berkeley, United States
Figures
Figure 1 with 3 supplements
A mechanical stiffness gradient in the follicle basement membrane.
(A) Elongation of the Drosophila follicle during oogenesis involves three components: the luminal germline, a surrounding epithelium, and an encasing basement membrane (BM) (see also Figure 1—figure supplement 1). Aspect ratios of stage 3, 5, and 7 egg chambers stained for DAPI (blue) and phalloidin (red), along with ColIV–GFP (green), are shown. (B) Atomic Force Microscopy (AFM) measurement of BM stiffness in living follicles. Absence of stroma and external position of BM allow direct access of the AFM probe. (C) Follicles are probed at different regions along the A–P axis, including the poles via Polydimethylsiloxane (PDMS) ‘egg cartons’. Stiffness measurements are derived from the first 50 nm of force–extension curves. (D) BM stiffness in the follicle center increases during development. Collagen digestion but not F-actin network disruption eliminates nearly all AFM-measured stiffness. (cf Figure 1—figure supplement 1). (E) Regional BM stiffness along the follicle A–P axis; color intensity matches position as in(C). WT follicles develop an A–P symmetrical gradient of mechanical anisotropy. Anterior and posterior poles are not distinguished. (F) fat2- and msn-depleted follicle BMs do not increase stiffness during development and remain mechanically isotropic. Scale bar: 25 µm.
Figure 1—figure supplement 1
Isotropic mechanical properties of cells in the Drosophila ovary.
(A,B) Cross-section of the acinus-like Drosophila follicle; planar epithelial and luminal expansionary forces, as well as basement membrane-based resistance, are diagrammed. (C–E) As compared to the elongation of growing WT follicles (C), growth of follicles following ablation of epithelium (tjGAL4 GAL80ts>Diptheria toxin A chain [D]) is isotropic. Note the absence of epithelium-produced BM (inset). The aspect ratio is quantitated in (E). (F) Assessment of cortical tension in follicle epithelial cells using laser nanodissection (red) and Myo:GFP localization (blue). (G) Severing of A–P and circumferential cell junctions at anterior, center, and posterior positions results in comparable recoil velocities. Example A–P and circumferential cuts in G’ and G’’ are shown. (H) Junctional non-muscle MyoII (Myo:GFP) localization is equivalent along A–P and circumferential cell junctions. Representative example in H’. Scale bars: 25 µm in (A–C), 5 µm inset in (G’,H’).
Figure 1—figure supplement 2
AFM elasticity measurement method.
(A) Follicles are indented to generate extension–deflection curves. Only the first 50 nm of deflection (plus 50 nm pre-contact) are used to fit for the Young’s modulus. Four curves are generated per position, averaged, then compared between A–P positions. (B) Indentation piezo (extension) speed optimization. Reduced stiffness at high speeds (0.8–1.0 µm/s) are indicative of viscoelasticity. 0.4 µm/s provided optimal elasticity accuracy and measurement speed.
Figure 1—figure supplement 3
Validation of pharmacological and hypertonic shock treatments for BM stiffness.
(A) Collagenase treatment of follicles prior to AFM does not disrupt cell–cell junctions, as monitored by E-cadherin–GFP. (B) Latrunculin A treatment of follicles prior to AFM effectively displaces Myo:GFP. (C) Hypertonic shrinkage of WT stage 7–8 follicles causes a significant reduction in size, but no significant loss of BM stiffness. Scale bar: 20 µm.
Figure 2
Manipulating the BM stiffness gradient alters organ shape.
For each follicle genotype, AFM-measured positional stiffness at stages 7–8 is shown above and degree of elongation is shown below. Manipulations in (A–F) alter gene expression uniformly via tjGAL4 (I) or homozygous genotype, whereas those in (G, H) alter gene expression regionally using centrally expressed mirGAL4 or terminally expressed fruGAL4 (J, K). Compared to WT (A), depletion of SPARC (B) softens the BM but preserves the anisotropic gradient; follicles elongate comparably to WT. Depletion of Collagen IV (ColIV) throughout the epithelium (C) creates a uniformly soft follicle with severe elongation defects, resembling mutants in which msn is depleted (D) or fat2 mutants (E). EHBP1 overexpression (F) increases stiffness while retaining an anisotropic gradient, and follicles hyperelongate. Depletion of Col IV in the central region alone (G) flattens the gradient while leaving terminal stiffness intact; this results in elongation defects. EHBP1 overexpression in the terminal regions alone (H) also flattens the gradient and results in elongation defects. (L) Aspect ratio vs stiffness anisotropy (defined as the ratio of central stiffness to the mean stiffness throughout the A–P axis) for genotypes (A–H) and for tj>DomeDN and tj>PerlOE.
Figure 3
The BM stiffness gradient creates anisotropic resistance to organ expansion.
(A) Design of osmotic-swelling experiments. Immersion in water causes influx (blue arrow) into the follicle (diagrammed in cross-section), resulting in increased turgor pressure (red arrows) that is resisted by the BM (green) as the organ swells. (B) WT follicle expressing ColIV–GFP, 1 min and 24 min after immersion (cf. Video 1). Position of the BM breach is indicated by the yellow arrowhead. (C) Frequency of follicle BM failure by stage and genotype, along with timing (D) of failure. WT BMs accommodate expansion with increasing efficiency as development proceeds in a manner independent of cellular F-actin; fat2 and collagenased follicles burst frequently and rapidly. (E) Position of BM failure: WT BMs breach most frequently at the poles, whereas fat2 and collagenased follicles also breach in other regions. (F) Frequency of BM failure in manipulated stage 7–8 follicles and (G) aspect ratio immediately before bursting. Scale bar: 25 µm.
Figure 4
Uniform circumferential mechanics in elongating follicles.
(A) ‘Unrolling’ of organ surface by ImSAnE allows quantitation of BM components along both A–P and circumferential axes. Image taken from Chen et al. (2016). (B) Analysis of BM fibril PCP shows WT polarity when Perl or DomeDN are overexpressed or when SPARC is depleted, contrasting with altered polarity in fat2 and absence of polarity in Col IV-depleted mutants. (C, D) Unrolling reveals increased variance in circumferential Col IV levels in fat2 as compared to those in WT or Perl-overexpressing follicles. The heat map indicates lowest (blue) to highest (red) intensities over equivalent ~35% circumferential segments. (E, F) AFM analysis along the circumferential axis of a follicle at a single central meridian. fat2 mutant follicles show high variability in BM stiffness, compared to the consistent values of WT or Perl-overexpressing follicles. Scale bars: 5 µm (B) and 10 µm (C).
Figure 5 with 3 supplements
Morphogen-like signaling creates the stiffness gradient.
Expression of GFP protein traps in BM components, assessed in WT stage 7–8 follicles that are physically flattened for visualization: (A) ColIV, (B) aminin B1, and (C) Perlecan. Heat maps indicate lowest (blue) to highest (red) intensities. The A–P ColIV pattern is disrupted in stage 7–8 follicles mutant for fat2 ([D], cf. Figure 5—figure supplement 1) or with inhibited JAK/STAT signaling (tj>domeDN, [E]) (cf. Figure 5—figure supplement 2). (F) Col IV transcription (ColIV-LacZ reporter expression) is not elevated in the central follicle. (G) Uniform production of ColIV (via hsFLP; act>y+>GAL4 UAS-myr-RFP) throughout the follicle (G’) results in elevated central incorporation. (H) ImSAnE ‘unrolling’ of the ColIV–GFP expressing follicle surface allows quantitation of intensity along the entire A–P axis; note the shorter axis of ‘round’ genotypes. (I) Along the A–P axis, ColIV levels are significantly elevated in the central region of WT and Perl-overexpressing follicles but not of fat2 or domeDN-expressing follicles. (J) Elongation failure is induced by inhibition of JAK-STAT signaling or by overexpression of Perl in follicles. (K) AFM reveals that follicles with inhibited JAK-STAT signaling or Perl overexpression do not develop an A–P stiffness gradient; Perl overexpressing follicles are softer than WT follicles. (L) Perl-overexpressing follicles burst easily under osmotic challenge, whereas follicles with inhibited JAK-STAT signaling are more similar to WT. Scale bars: 25 µm (A–G’) and 10 µm (H).
Figure 5—figure supplement 1
fat2KO phenocopies other fat2 null alleles.
(A) Loss of basal actin PCP, (B) elongation defects, (C) Collagen IV–GFP pattern (compare to Figure 6D) and (D) bursting frequency in distilled water are indistinguishable between fat2KO and the well-characterized EMS-generated null allele fat258D. Scale bars: 10 µm (A) and 20 µm (C).
Figure 5—figure supplement 2
STAT reporter in fat2 mutants.
(A) fat2 loss does not disrupt A–P patterning as detected by the 10XSTAT–GFP reporter. Scale bar: 20 µm.
Figure 5—figure supplement 3
BM stiffness and active follicle rotation.
Depletion of actin regulator Abi following stage 5 (A) halts rotation but (B) does not soften BM at stage 7–8 nor (C) alter bursting characteristics at stage 7–8; (D) follicles show normal elongation at stage 7–8 (cf. Cetera and Horne-Badovinac, 2015).
Author response image 1
(A) St. 7-8 follicles were indented with a 10µm bead-tipped cantilever.
Relative stiffness differences between A-P position were similar to pyramidal-tipped cantilevers. N=14 follicles. (B) St. 10 follicles (N=11) were indented and showed gradient of stiffness as in st. 7-8 (N=10), however the anterior region becomes significantly softer. (C) Final egg shape of selected genotypes. With the exception, of Fru>Ehbp1OE, all genotypes had defective follicle and egg elongation. N>= 20 eggs each. (D) Hypertonic media (2000mOsm) containing Sorbitol was used to reduce follicle osmotic pressure. Basement membrane stiffness was measured in the center of st. 7-8 follicles and was not significantly different when cultured in Sorbitol media (N= 16) compared to standard media (N=16). It is worth noting that only a very slight reduction in follicle midsagittal area was achieved with a variety of hypertonic treatments making significant conclusions problematic. (E) short egg (seg, N=63) osmotic bursting was not significantly different from WT (N=80).
Videos
Video 1
WT Follicle swelling in H2O.
Bursting of WT follicles when placed in water as shown in Figure 4B. Follicle nuclei are visualized using histone–mRFP, and BM is labeled with ColIV–GFP fluorescence (green).
Video 2
fat2 follicle swelling in H2O.
Rapid bursting of fat2 follicles when placed in water as quantified in Figure 4D. The follicle is visualized using FM4-64, and BM is labeled with ColIV–GFP fluorescence (green).
Video 3
Osmotic bursting of manipulated genotypes placed in water.
As quantified in Figure 4E–G, compared to WT, fat2 follicles burst rapidly and often not at the poles, whereas follicles uniformly overexpressing EHBP1 (tj>EHBP1) swell anisotropically and do not burst at all. Overexpressing EHBP1 in poles (fru>EHBP1) induces generally isotropic swelling but also prevents bursting. Depleting Coll IV in the central region (mirr>Col IV KD) cause isotropic swelling and central bursting.
Video 4
Follicle rotation in manipulated genotypes.
Rotation of tj>Perl and tj>Dome-DN is comparable to that of WT, whereas tj>abi-RNAi initiated at stage 5 blocks rotation. Scale bar: 10 µm.
Additional files
-
Source code 1
AFM curve fitting.
- https://doi.org/10.7554/eLife.24958.018
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Supplementary file 1
Experimental genotypes.
- https://doi.org/10.7554/eLife.24958.019
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Organ sculpting by patterned extracellular matrix stiffness
eLife 6:e24958.
https://doi.org/10.7554/eLife.24958
